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    • 2. 发明授权
    • Affinity membrane for capture of a target biomolecule and formation thereof by site-directed immobilization of a capture biomolecule
    • 用于捕获靶生物分子的亲和膜及其通过捕获生物分子的定点固定形成
    • US07771955B2
    • 2010-08-10
    • US11447154
    • 2006-06-06
    • Timothy Alan BarbariSufi Rizwan Ahmed
    • Timothy Alan BarbariSufi Rizwan Ahmed
    • G01N33/53C07F15/04C12P21/02
    • C07K17/06G01N33/54353G01N33/545
    • Compositions and methods are taught for directing the orientation of an immobilized capture biomolecule on a hydrophobic membrane. The method comprises layering at least one tie layer on a hydrophobic membrane, adding an amine functional layer on top of at least one tie layer; and attaching an alignment biomolecule to the amine functional layer. The alignment biomolecule has the ability to either capture a target biomolecule itself and thus be considered a capture biomolecule, or bind and orient the immobilized capture biomolecule so as to maximize the binding activity of the immobilized capture biomolecule. In one embodiment, a nickel-coordinated amine functional layer binds with a histidine-tagged alignment biomolecule. In another embodiment, an amine functional layer reacts, via tyrosinase catalysis, with a tyrosine residue in an alignment biomolecule.
    • 教导组合物和方法将固定的捕获生物分子的取向引导到疏水膜上。 该方法包括在疏水膜上层叠至少一个粘结层,在至少一个粘结层的顶部上加入胺官能层; 并将取向生物分子附着到胺官能层上。 取向生物分子具有捕获目标生物分子本身的能力,因此被认为是捕获生物分子,或者结合和定向固定的捕获生物分子,以便使固定的捕获生物分子的结合活性最大化。 在一个实施方案中,镍配位的胺功能层与组氨酸标记的取向生物分子结合。 在另一个实施方案中,胺功能层通过酪氨酸酶催化与对准生物分子中的酪氨酸残基反应。